Package 71872-7247-1

Brand: sodium bicarbonate

Generic: sodium bicarbonate
NDC Package

Package Facts

Identity

Package NDC 71872-7247-1
Digits Only 7187272471
Product NDC 71872-7247
Description

1 VIAL, SINGLE-DOSE in 1 BAG (71872-7247-1) / 50 mL in 1 VIAL, SINGLE-DOSE

Marketing

Marketing Status
Marketed Since 2021-03-30
Brand sodium bicarbonate
Generic sodium bicarbonate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "bfc9bcd9-4b2f-ce7e-e053-2995a90a6cd1", "openfda": {"unii": ["8MDF5V39QO"], "rxcui": ["1868486"], "spl_set_id": ["bfc9c321-665c-ca97-e053-2995a90a7954"], "manufacturer_name": ["Medical Purchasing Solutions, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 BAG (71872-7247-1)  / 50 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "71872-7247-1", "marketing_start_date": "20210330"}], "brand_name": "SODIUM BICARBONATE", "product_id": "71872-7247_bfc9bcd9-4b2f-ce7e-e053-2995a90a6cd1", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Increased Large Intestinal Motility [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]"], "product_ndc": "71872-7247", "generic_name": "SODIUM BICARBONATE", "labeler_name": "Medical Purchasing Solutions, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "SODIUM BICARBONATE", "active_ingredients": [{"name": "SODIUM BICARBONATE", "strength": "84 mg/mL"}], "application_number": "ANDA202432", "marketing_category": "ANDA", "marketing_start_date": "20210301", "listing_expiration_date": "20261231"}